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High-resolution HLA-DRB1 genotyping in an Australian inclusion body myositis (s-IBM) cohort: an analysis of disease-associated alleles and diplotypes.
Rojana-udomsart A, James I, Castley A, Needham M, Scott A, Day T, Kiers L, Corbett A, Sue C, Witt C, Martinez P, Christiansen F, Mastaglia F. Rojana-udomsart A, et al. Among authors: corbett a. J Neuroimmunol. 2012 Sep 15;250(1-2):77-82. doi: 10.1016/j.jneuroim.2012.05.003. Epub 2012 May 26. J Neuroimmunol. 2012. PMID: 22633068
Expanding the phenotype of GMPPB mutations.
Cabrera-Serrano M, Ghaoui R, Ravenscroft G, Johnsen RD, Davis MR, Corbett A, Reddel S, Sue CM, Liang C, Waddell LB, Kaur S, Lek M, North KN, MacArthur DG, Lamont PJ, Clarke NF, Laing NG. Cabrera-Serrano M, et al. Among authors: corbett a. Brain. 2015 Apr;138(Pt 4):836-44. doi: 10.1093/brain/awv013. Epub 2015 Feb 12. Brain. 2015. PMID: 25681410
Mortality and Causes of Death in Patients with Sporadic Inclusion Body Myositis: Survey Study Based on the Clinical Experience of Specialists in Australia, Europe and the USA.
Price MA, Barghout V, Benveniste O, Christopher-Stine L, Corbett A, de Visser M, Hilton-Jones D, Kissel JT, Lloyd TE, Lundberg IE, Mastaglia F, Mozaffar T, Needham M, Schmidt J, Sivakumar K, DeMuro C, Tseng BS. Price MA, et al. Among authors: corbett a. J Neuromuscul Dis. 2016 Mar 3;3(1):67-75. doi: 10.3233/JND-150138. J Neuromuscul Dis. 2016. PMID: 27854208 Free PMC article.
Sarcolemmal excitability in the myotonic dystrophies.
Boland-Freitas R, Lee J, Howells J, Liang C, Corbett A, Nicholson G, Ng K. Boland-Freitas R, et al. Among authors: corbett a. Muscle Nerve. 2018 Apr;57(4):595-602. doi: 10.1002/mus.25962. Epub 2017 Sep 30. Muscle Nerve. 2018. PMID: 28881011
756 results